A new look towards BAC-based array CGH through a comprehensive comparison with oligo-based array CGH

被引:27
作者
Wicker, Nicolas
Carles, Annaick
Mills, Ian G.
Wolf, Maija
Veerakumarasivam, Abhi
Edgren, Henrik
Boileau, Fabrice
Wasylyk, Bohdan
Schalken, Jack A.
Neal, David E.
Kallioniemi, Olli
Poch, Olivier
机构
[1] Inst Genet & Biol Mol & Cellulaire, Lab Bioinformat & Genom Integrat, F-67404 Illkirch Graffenstaden, France
[2] Li Ka Shing Ctr, Cambridge Res Inst, Canc Res UK, Urooncol Res Grp, Cambridge CB2 0RE, England
[3] VTT Tech Res Ctr Finland, FIN-20520 Turku, Finland
[4] Univ Turku, FIN-20520 Turku, Finland
[5] Univ Cambridge, Hutchison Med Res Council Canc Res Ctr, Dept Oncol, Canc Res UK Urooncol Res Grp, Cambridge CB2 2XZ, England
[6] Inst Genet & Biol Mol & Cellulaire, F-67404 Illkirch Graffenstaden, France
[7] Univ Amsterdam, Acad Med Ctr, Dept Urol G4 105 1, NL-1105 AZ Amsterdam, Netherlands
来源
BMC GENOMICS | 2007年 / 8卷
关键词
DNA COPY-NUMBER; COMPARATIVE-GENOMIC-HYBRIDIZATION; HUMAN NEOPLASMS; CELL LYMPHOMA; MICROARRAYS; AMPLIFICATIONS; CANCER; TUMORS;
D O I
10.1186/1471-2164-8-84
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Currently, two main technologies are used for screening of DNA copy number; the BAC ( Bacterial Artificial Chromosome) and the recently developed oligonucleotide-based CGH ( Chromosomal Comparative Genomic Hybridization) arrays which are capable of detecting small genomic regions with amplification or deletion. The correlation as well as the discriminative power of these platforms has never been compared statistically on a significant set of human patient samples. Results: In this paper, we present an exhaustive comparison between the two CGH platforms, undertaken at two independent sites using the same batch of DNA from 19 advanced prostate cancers. The comparison was performed directly on the raw data and a significant correlation was found between the two platforms. The correlation was greatly improved when the data were averaged over large chromosomic regions using a segmentation algorithm. In addition, this analysis has enabled the development of a statistical model to discriminate BAC outliers that might indicate microevents. These microevents were validated by the oligo platform results. Conclusion: This article presents a genome-wide statistical validation of the oligo array platform on a large set of patient samples and demonstrates statistically its superiority over the BAC platform for the Identification of chromosomic events. Taking advantage of a large set of human samples treated by the two technologies, a statistical model has been developed to show that the BAC platform could also detect microevents.
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页数:10
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